Canonical Allele Identifier: PA915989937
Gene: IDS HGNC NCBI

Linked Data

ClinVar Variation Id: 221206
ClinVar RCV Id: RCV000205759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001160022.1:p.Pro30His
CA349872
NM_001166550.4:c.89C>A